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抗肿瘤药物黄绿青霉素的生物合成涉及蒽环聚酮类化合物的氧化重排。

Biosynthesis of the antitumor agent chartreusin involves the oxidative rearrangement of an anthracyclic polyketide.

作者信息

Xu Zhongli, Jakobi Kathrin, Welzel Katrin, Hertweck Christian

机构信息

Leibniz-Institute for Natural Products Research and Infection Biology, HKI, Department of Bioorganic Synthesis, Beutenbergstrasse 11a, D-07745 Jena, Germany.

出版信息

Chem Biol. 2005 May;12(5):579-88. doi: 10.1016/j.chembiol.2005.04.017.

Abstract

Chartreusin is a potent antitumor agent with a mixed polyketide-carbohydrate structure produced by Streptomyces chartreusis. Three type II polyketide synthase (PKS) gene clusters were identified from an S. chartreusis HKI-249 genomic cosmid library, one of which encodes chartreusin (cha) biosynthesis, as confirmed by heterologous expression of the entire cha gene cluster in Streptomyces albus. Molecular analysis of the approximately 37 kb locus and structure elucidation of a linear pathway intermediate from an engineered mutant reveal that the unusual bis-lactone aglycone chartarin is derived from an anthracycline-type polyketide. A revised biosynthetic model involving an oxidative rearrangement is presented.

摘要

杀念珠菌素是一种由白色链霉菌产生的具有混合聚酮化合物-碳水化合物结构的强效抗肿瘤剂。从白色链霉菌HKI-249基因组粘粒文库中鉴定出三个II型聚酮化合物合酶(PKS)基因簇,其中一个编码杀念珠菌素(cha)的生物合成,这通过在白色链霉菌中对整个cha基因簇的异源表达得到证实。对大约37 kb位点的分子分析以及对工程突变体的线性途径中间体的结构解析表明,不寻常的双内酯苷元杀念珠菌素源自蒽环类聚酮化合物。提出了一个涉及氧化重排的修订生物合成模型。

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